Disruption of heparan sulfate proteoglycan conformation perturbs B-cell maturation and APRIL-mediated plasma cell survival

Author:

Reijmers Rogier M.1,Groen Richard W. J.1,Kuil Annemieke1,Weijer Kees2,Kimberley Fiona C.3,Medema Jan Paul3,van Kuppevelt Toin H.4,Li Jin-Ping5,Spaargaren Marcel1,Pals Steven T.1

Affiliation:

1. Department of Pathology,

2. Department of Cell Biology and Histology, and

3. Laboratory of Experimental Oncology, Academic Medical Center, Amsterdam, The Netherlands;

4. Department of Biochemistry, NCMLS, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands; and

5. Department of Medical Biochemistry and Microbiology, University of Uppsala, Uppsala, Sweden

Abstract

Abstract The development and antigen-dependent differentiation of B lymphocytes are orchestrated by an array of growth factors, cytokines, and chemokines that require tight spatiotemporal regulation. Heparan sulfate proteoglycans specifically bind and regulate the bioavailability of soluble protein ligands, but their role in the immune system has remained largely unexplored. Modification of heparan sulfate by glucuronyl C5-epimerase (Glce) controls heparan sulfate-chain flexibility and thereby affects ligand binding. Here we show that Glce deficiency impairs B-cell maturation, resulting in decreased plasma cell numbers and immunoglobulin levels. We demonstrate that C5-epimerase modification of heparan sulfate is critical for binding of a proliferation inducing ligand (APRIL) and that Glce-deficient plasma cells fail to respond to APRIL-mediated survival signals. Our results identify heparan sulfate proteoglycans as novel players in B-cell maturation and differentiation and suggest that heparan sulfate conformation is crucial for recruitment of factors that control plasma cell survival.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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